Thermopsis lanceolata - Unknown
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Internal ID UUID643fdf1edc2cc561079078
Scientific name Thermopsis lanceolata
Authority R.Br.
First published in W.T.Aiton, Hortus Kew.3: 3 (1811)

Description Top

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Thermopsis lanceolata, also known as the tapered false lupin, is a species of flowering plant in the legume family Fabaceae. It is native to Russia, Kazakhstan, Mongolia, Nepal, and China. Growing to 1 m tall and broad, this herbaceous perennial has grey-green leaves and erect tapering panicles of pale yellow, pea-like flowers in spring. It is closely related to the familiar lupins of gardens, but with a more bushy appearance. The Latin specific epithet lanceolata means 'spear-shaped', in reference to the leaves. The plant is tough and resilient, tolerating a wide range of growing conditions, but resents disturbance.

Synonyms Top

Scientific name Authority First published in
Thermopsis lupinoides (L.) Link Enum. Hort. Berol. Alt.1: 401 (1821)
Thermopsis fabacea (Pall.) DC. Prodr.2: 99 (1825)
Sophora fabacea Pall. Sp. Astragal.: 122 (1800)
Sophora lupinoides L. Sp. Pl.: 374 (1753)
Thermopsis lanceolata var. lanceolata R.Br.
Thermopsis sibirica Czefr. Novosti Sist. Vyssh. Rast.13: 180 (1976)
Thermopsis lanceolata var. glabra (Czefr.) Kurbatski
Thermopsis glabra Czefr. Novosti Sist. Vyssh. Rast.13: 182 (1976)
Thermopsis orientalis Czefr. Novosti Sist. Vyssh. Rast.13: 188 (1976)
Thermia fabacea (Pall.) Spreng. Syst. Veg. ed. 16, 4(2): 171 (1827)
Thermia lupinoides Nutt. Gen. N. Amer. Pl.1: 283 (1818)
Podalyria lupinoides (L.) Lam. Tabl. Encycl.2: 471 (1793)
Baptisia lupinoides (L.) Burb. Gard. Chron., n.s., 21: 827 (1884)
Thermopsis lanceolata subsp. glabra (Czefr.) Kurbatski Sibir. Biol. Zhurn.1991(3): 35 (1991)
Thermopsis lanceolata var. glabra (Czefr.) Yakovlev Novosti Sist. Vyssh. Rast.15: 171 (1979)
Thermopsis lanceolata subsp. sibirica (Czefr.) Kurbatski Sibir. Biol. Zhurn.1991(3): 35 (1991)

Common names Top

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Language Common/alternative name
Azerbaijani nəştərvari termopsis
Finnish aasianrevonpapu
Kazakh Қандауыр тентекмия
Yakutian Итирдэр от
Chinese 披针叶野决明
Chinese 披针叶黄华
Chinese 披针叶黄花
Chinese 牧马豆
Chinese 牧马豆根
Chinese 野决明
Chinese 披針葉野决明

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Resents Transplanting: These plants do not tolerate the disturbance of their roots well. It's best to sow these seeds in their final growing location or in a container from which they can be moved without disturbing the root ball.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
tiny seed should be scarified with sandpaper

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Kamchatka
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin
    • Siberia
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000213939
Tropicos 13033626
KEW urn:lsid:ipni.org:names:521187-1
The Plant List ild-9001
Open Tree Of Life 356276
Observations.org 131296
NCBI Taxonomy 114320
IPNI 521187-1
iNaturalist 466078
GBIF 5360203
EPPO THRLA
EOL 704093
Elurikkus 527835
USDA GRIN 36517
Wikipedia Thermopsis_lanceolata
CMAUP NPO16775

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
A dataset for fine-grained seed recognition Yuan M, Lv N, Dong Y, Hu X, Lu F, Zhan K, Shen J, Wu X, Zhu L, Xie Y Sci Data 06-Apr-2024
PMCID:PMC10998916
doi:10.1038/s41597-024-03176-5
PMID:38582756
Response of species dominance and niche of plant community to wetland degradation along alpine lake riparian Wu S, Dong S, Wang Z, Li S, Ma C, Li Z Front Plant Sci 25-Mar-2024
PMCID:PMC10999619
doi:10.3389/fpls.2024.1352834
PMID:38590743
The complete chloroplast genome sequence of Ammodendron bifolium (Fabaceae), an endangered desert shrub from China Tian H, Zhu X, Qiu J, Zhang H, Shi X Mitochondrial DNA B Resour 03-Mar-2024
PMCID:PMC10913713
doi:10.1080/23802359.2024.2324922
PMID:38450410
Unveiling the potential anti‐cancer activity of calycosin against multivarious cancers with molecular insights: A promising frontier in cancer research Sohel M, Zahra Shova FT, shuvo S, Mahjabin T, Mojnu Mia M, Halder D, Islam H, Roman Mogal M, Biswas P, Saha HR, Sarkar BC, Mamun AA Cancer Med 17-Jan-2024
PMCID:PMC10905684
doi:10.1002/cam4.6924
PMID:38230908
Indirect regulation of topsoil nutrient cycling by groundwater depth: impacts on sand-fixing vegetation and rhizosphere bacterial communities Hao L, Liu X, Ji R, Ma Y, Wu P, Cao Q, Xin Y Front Microbiol 05-Dec-2023
PMCID:PMC10746847
doi:10.3389/fmicb.2023.1285922
PMID:38143862
Effects of Different Livestock Grazing on Foliar Fungal Diseases in an Alpine Grassland on the Qinghai–Tibet Plateau Tian Z, Li W, Kou Y, Dong X, Liu H, Yang X, Dong Q, Chen T J Fungi (Basel) 20-Sep-2023
PMCID:PMC10533196
doi:10.3390/jof9090949
PMID:37755057
Advances in research and utilization of botanical pesticides for agricultural pest management in Inner Mongolia, China Guo C, Wang L, Chen N, Zhang M, Jia J, Lv L, Li M Chin Herb Med 28-Aug-2023
PMCID:PMC11064588
doi:10.1016/j.chmed.2023.04.002
PMID:38706822
Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity Cely-Veloza W, Kato MJ, Coy-Barrera E ACS Omega 28-Jul-2023
PMCID:PMC10413377
doi:10.1021/acsomega.3c02179
PMID:37576649
Response mechanisms of 3 typical plants nitrogen and phosphorus nutrient cycling to nitrogen deposition in temperate meadow grasslands Zhang Y, Zhang Q, Yang W, Zhang Y, Wang N, Fan P, You C, Yu L, Gao Q, Wang H, Zheng P, Wang R Front Plant Sci 07-Jul-2023
PMCID:PMC10361690
doi:10.3389/fpls.2023.1140080
PMID:37484465
Food production and agricultural systems on the southwestern frontier of the Han Empire: archaeobotanical remains from the 2016 excavation of Hebosuo, Yunnan Yang W, Jiang Z, Yao A, Dal Martello R, Jiang J, Xie H, Chen X Archaeol Anthropol Sci 04-May-2023
PMCID:PMC10160161
doi:10.1007/s12520-023-01766-9
PMID:37159718
Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments Zhou Y, Wang D, Yan W Nutrients 18-Feb-2023
PMCID:PMC9967064
doi:10.3390/nu15041031
PMID:36839389
Synthesis, Properties and Spatial Structure of 4-[(3,5-Dimethyl-1,2-oxazol-4-yl)sulfonyl]cytisine Ibrayev MK, Nurkenov OA, Rakhimberlinova ZB, Takibayeva AT, Turdybekov DM, Seilkhanov TM, Issabayeva MB, Kelmyalene AA, Kezdikbayeva AT, Mendibayeva AZ Plants (Basel) 27-Dec-2022
PMCID:PMC9823373
doi:10.3390/plants12010137
PMID:36616266
The complete chloroplast genome of Thermopsis lanceolata: genome structure and its phylogenetic relationships within the family Fabaceae Dorjee T, Gao F, Zhou Y Mitochondrial DNA B Resour 12-Dec-2022
PMCID:PMC9754016
doi:10.1080/23802359.2022.2154623
PMID:36530460
Comparison of Root Ecological Stoichiometry between Non-Growing Season and Growing Season of Grassland on the Chang Tang Plateau Ma X, Yan Y, Hong J, Wang X Int J Environ Res Public Health 08-Nov-2022
PMCID:PMC9689994
doi:10.3390/ijerph192214628
PMID:36429348
Ecological Niche and Interspecific Association of Plant Communities in Alpine Desertification Grasslands: A Case Study of Qinghai Lake Basin Hu Y, Wang H, Jia H, Pen M, Liu N, Wei J, Zhou B Plants (Basel) 15-Oct-2022
PMCID:PMC9609917
doi:10.3390/plants11202724
PMID:36297752

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
13-Acetoxyanagyrine 156996 Click to see CC(=O)OC1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 302.37 unknown via CMAUP database
7,14-Methano-4H,6H-dipyrido[1,2-a:1',2'-E][1,5]diazocin-4-one, 7,7a,8,9,10,11,13,14-octahydro-, [7R-(7alpha,7aalpha,14alpha)]- 91746595 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(00)84121-7
Anagyrin 71056954 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(00)84121-7
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/S0031-9422(00)84121-7
(1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one 1278189 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1007/BF00564734
(1S,5R)-3,4,5,6-tetrahydro-1H-1,5-methanopyrido[1,2-a][1,5]diazocin-8(2H)-one 6713952 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown via CMAUP database
(1S,9R)-11-but-3-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 7067420 Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2 244.33 unknown via CMAUP database
11-(6-Oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-diene-11-carbonyl)-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 4486244 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C(=O)N4CC5CC(C4)C6=CC=CC(=O)N6C5 406.50 unknown via CMAUP database
Citizin 22407 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1007/BF00565346
https://doi.org/10.1007/BF00564734
Cytisine, N-formyl- 589870 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1016/S0031-9422(00)84121-7
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1007/BF00564734
https://doi.org/10.1007/BF00565346
N-Methylcytisine 234566 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1007/BF00564734
Pharmakon1600-01504027 6708720 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(00)84121-7
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,9R,10R)-5-[(1S,9S,10R)-6-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-3-yl]-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 162984954 Click to see C1CCN2CC3CC(C2C1)CN4C3=C(CCC4=O)C5=CC=C6C7CC(CN6C5=O)C8CCCCN8C7 488.70 unknown https://doi.org/10.1007/BF00564446
5-(6-Oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-3-yl)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 12309279 Click to see C1CCN2CC3CC(C2C1)CN4C3=C(CCC4=O)C5=CC=C6C7CC(CN6C5=O)C8CCCCN8C7 488.70 unknown https://doi.org/10.1007/BF00564446
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/S0031-9422(00)84121-7
Lupanine(1+) 6987464 Click to see C1CC[NH+]2CC3CC(C2C1)CN4C3CCCC4=O 249.37 unknown via CMAUP database
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown via CMAUP database
Tetrahydrodeoxoargentamin 261946 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(CC4)O 250.38 unknown https://doi.org/10.1016/S0031-9422(00)84121-7
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3R,4S,4aR,10bR)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 6543710 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O 328.27 unknown via CMAUP database
> Hydrocarbon derivatives / Tropones
Gloriosine 23890 Click to see COC1=CC=C2C(=CC1=O)C(CCC3=CC(=C(C(=C32)OC)OC)OC)NC=O 385.40 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Ethane 6324 Click to see CC 30.07 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
dimethyl (5R,5'S,6R,8S)-8-acetyloxy-5'-(furan-3-yl)-6-methyl-2'-oxospiro[2,3,4,6,7,8-hexahydronaphthalene-5,3'-oxolane]-1,1-dicarboxylate 101316809 Click to see CC1CC(C2=C(C13CC(OC3=O)C4=COC=C4)CCCC2(C(=O)OC)C(=O)OC)OC(=O)C 460.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(13alpha)-3alpha-(Benzoyloxy)-12beta-hydroxyursane-28-oic acid 28,12-lactone 100973316 Click to see CC1CCC23CCC4(C(C2C1C)C(CC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C7=CC=CC=C7)C)C)OC3=O)C 560.80 unknown via CMAUP database
(13alpha)-3alpha-Hydroxyursan-28-oic acid 100973318 Click to see CC1CCC2(CCC3(C(C2C1C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O 458.70 unknown via CMAUP database
(1R,3aR,5aR,5bR,7aS,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 7092625 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
(1R,4S,5S,8S,9R,10S,13S,14R,16R,17S,22R)-8-hydroxy-4,9,10,14,17,20,20-heptamethyl-24-oxahexacyclo[14.6.2.01,14.04,13.05,10.017,22]tetracosan-23-one 11070498 Click to see CC1C(CCC2C1(CCC3C2(CCC45C3(CC(C6(C4CC(CC6)(C)C)C)OC5=O)C)C)C)O 456.70 unknown via CMAUP database
(1R,4S,5S,9R,10S,13S,14R,16R,17S,22R)-4,9,10,14,17,20,20-heptamethyl-24-oxahexacyclo[14.6.2.01,14.04,13.05,10.017,22]tetracosane-8,23-dione 10928543 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC45C3(CC(C6(C4CC(CC6)(C)C)C)OC5=O)C)C)C 454.70 unknown via CMAUP database
(3aR,5aR,5bR,7aR,11aR,11bR,13aS)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-3,4,5,6,7,7a,10,11,11b,12,13,13a-dodecahydro-2H-cyclopenta[a]chrysen-9-one 17751023 Click to see CC(C)C1=C2C3CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1)C)C)C)(C)C)C 424.70 unknown via CMAUP database
[(1S,4R,5R,8R,10R,13R,14R,16R,17S,18S,19S,20R,23R)-23-methoxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[14.6.2.01,18.04,17.05,14.08,13]tetracosan-10-yl] benzoate 100973317 Click to see CC1CCC23CCC4(C(C2C1C)C(CC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C7=CC=CC=C7)C)C)OC3OC)C 576.80 unknown via CMAUP database
3alpha-(Benzoyloxy)-16alpha-hydroxy-D:A-friedoolean-27-oic acid 27,16-lactone 11060762 Click to see CC1C(CCC2C1(CCC3C2(CCC45C3(CC(C6(C4CC(CC6)(C)C)C)OC5=O)C)C)C)OC(=O)C7=CC=CC=C7 560.80 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Methyl Ursolate 636516 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Odoroside F 120681 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC7C(C(C(C(O7)CO)O)O)O)OC)O 696.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2,4,5,6-tetrahydro-1H-cyclopenta[d][1,3]oxazin-7-one 5316289 Click to see C1CC(=O)C2=C1COCN2 139.15 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Teucvin 179592 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown via CMAUP database
Teuflin 13071598 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / 3-pyridinecarbonitriles
Mallorepine 13027 Click to see CN1C=CC(=O)C(=C1)C#N 134.14 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Dihydropyridines
1-Methyl-4-oxo-1,4-dihydropyridine-2-carbonitrile 45087607 Click to see CN1C=CC(=O)C=C1C#N 134.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(8Z)-8-[(2,3-dihydroxyphenyl)methylidene]pentadecan-7-one 5320983 Click to see CCCCCCCC(=CC1=C(C(=CC=C1)O)O)C(=O)CCCCCC 346.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Sparticarpin 442823 Click to see COC1=C(C=C2C(=C1)C3C(CO2)C4=C(O3)C=C(C=C4)O)OC 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 154496625 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00564317
> Phenylpropanoids and polyketides / Tannins
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(Z)-3-[(3S,4R)-3-carboxy-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromen-4-yl]-4-[[(1R,19R,21S,22R,23R)-6-(6-carboxy-2,3,4-trihydroxyphenoxy)-7,8,11,12,13,22-hexahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl]oxy]-4-oxobut-2-enoate 21672437 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)OC6=C(C(=C(C=C6C(=O)O)O)O)O)OC(=O)C(=CC(=O)[O-])C7C(OC(=O)C8=CC(=C(C(=C78)O)O)O)C(=O)O 1137.80 unknown via CMAUP database
(Z)-3-[(3S,4R)-3-carboxy-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromen-4-yl]-4-[[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl]oxy]-4-oxobut-2-enoate 21672435 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C(=CC(=O)[O-])C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O 969.60 unknown via CMAUP database
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown via CMAUP database
Eugeniin 442679 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown via CMAUP database
Mallotinic Acid 10056140 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)OC6=C(C(=C(C=C6C(=O)O)O)O)O)O 802.60 unknown via CMAUP database
Punicafolin 5320800 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 938.70 unknown via CMAUP database
Wutxioakrfkqhk-bwpkhyersa- 21672436 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C(=CC(=O)O)C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O 970.70 unknown via CMAUP database

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